inhousefyi
← Back to listings

Senior Principal Regulatory Affairs Specialist

BALT GroupIrvine, California, United States · Posted 5 months ago
Full-timeEst. 185,000 USD
Apply now

Description

About Balt

Our purpose is to improve the lives of 150,000 patients in 2026.

Our story

Balt is a rapidly growing pioneer in an exceptional field. For 45 years, Balt has been leading the way - collaborating with physicians and institutions to develop elegant medical devices. Our products are being used by physicians across the world, and we have 13 offices in 11 countries – and counting.

We introduced one of the first neurovascular intervention devices in 1977 and now offer the world's broadest portfolio of medical devices for stroke. As the premier global neurovascular platform always seeking to expand beyond boundaries, we are now bringing our innovation to the peripheral vascular space.

We are proud of our mission, our people, and the incredible work we accomplish together as we empower physicians to save lives.

Why Join Balt? Join a passionate team, dedicated to making a difference.

  1. Working at Balt means giving meaning to your work! Pride is a strong part of our identity.
  2. We are a close-knit team, with strong mission, vision and values that guide our day-to-day.
  3. Recognition of work, respect, and our multicultural community are key aspects of the employee experience and contribute to our continued success.
  4. No matter the country, we take care of you.

Would you like to be part of our story? Don't hesitate, come and join us!

About this opportunity – Senior Principal Regulatory Affairs Specialist

Description

The Sr. Principal Regulatory Affairs Specialist is a seasoned expert, responsible for completing and maintaining regulatory approvals/clearances for new and modified medical devices, license renewals, and annual registrations. Serves as a Regulatory representative on specific multi-discipline teams, responsible for organizing and leading meetings and acts independently to identify and resolve problems that may be complex in nature. Applies advanced regulatory expertise to guide cross-functional partners and demonstrates strategic thinking and creativity in support of projects. Interacts directly with regulatory bodies.

Job Responsibilities

  1. Develop and implement global regulatory strategies for complex, high-risk medical devices including contingency plans.
  2. Represent Regulatory Affairs on project teams and partners with cross-functional teams to ensure alignment of regulatory strategies and organizational objectives.
  3. Writes, reviews and files regulatory submissions and documentation for the US and internationally.
  4. Support product maintenance for currently marketed products, as necessary.
  5. Reviews device labeling for compliance with the applicable US and international regulations.
  6. Reviews product and manufacturing changes for compliance with applicable regulations.
  7. Reviews advertising and promotion to ensure compliance with product claims
  8. Documents, consolidates, and maintains verbal and written communication with regulatory agencies.
  9. Identify and evaluate regulatory processes and systems for improvements ensuring compliance
  10. Assists with audits and inspections, as needed
  11. Performs other duties and responsibilities as assigned.

Qualification Requirements

Skills:

  1. Experience in Humanitarian Device Exemption (HDE), Investigational Device Exemption (IDE), and Pre-Market Approval (PMA) applications
  2. Demonstrate strong project management, writing, coordination, and execution of regulatory items, with emphasis on technical and scientific regulatory activities.
  3. Ability to work well in a team environment.
  4. Works well under pressure in a dynamic, timeline-driven environment
  5. Demonstrated MS Office and Adobe Acrobat software skills

Pre-Requisites/Job Experience:

  1. Minimum BA/BS degree or higher in a scientific or technical discipline or relevant field of study.
  2. Nine (9) + years of professional regulatory experience.
  3. Documented experience in preparation of US and EU submissions
  4. Experience interfacing with relevant regulatory authorities through all stages of device life cycle.

Physical Requirements:

  1. Must be able to remain in a stationary position 50%
  2. Constantly operate a computer and other office equipment, such as copy machine, printer, etc.

Work Environment

Working conditions are normal for an office environment.

The above information on this description have been designed to indicate the general nature of work performed by employees within this position. It is not a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job.

Balt Group is an Equal Employment Opportunity employer.

More information please go to www.baltgroup.com

Please be aware of a current job offer scam perpetrated through the use of the internet. The scammers frequently misappropriate and use a company’s log and photos to give the appearance of legitimacy. The scam preys upon those seeking employment and uses false and fraudulent offers of employment with employers, such as Balt Inc to steal from the victims. Balt believes that one of the best ways to put a stop to this scam is to make sure you are aware of it. Balt’s job recruitment process involves live communication: in person, telephone, and/or video interviews in most cases.

#LI-FW1

Pay Range
$170,000$200,000 USD

Similar jobs

BALT GroupIrvine, California, United States

Est. 187,500 USD

About Balt Our purpose is to improve the lives of 150,000 patients in 2026. Our story Balt is a rapidly growing pioneer in an exceptional field. For 45 years, Balt has been leading the way - collaborating with physicians…

Full-time
BALT GroupBoston, Massachusetts, United States

Est. 262,500 USD

About Balt Our purpose is to improve the lives of 150,000 patients in 2026. Our story Balt is a rapidly growing pioneer in an exceptional field. For 45 years, Balt has been leading the way - collaborating with physicians…

Full-time
BALT GroupIrvine, California, United States

Est. 145,000 USD

About Balt Our purpose is to improve the lives of 150,000 patients in 2026. Our story Balt is a rapidly growing pioneer in an exceptional field. For 45 years, Balt has been leading the way - collaborating with physicians…

Full-time
BALT GroupIrvine, California, United States

Est. 145,000 USD

About Balt Our purpose is to improve the lives of 150,000 patients in 2026. Our story Balt is a rapidly growing pioneer in an exceptional field. For 45 years, Balt has been leading the way - collaborating with physicians…

Full-time
BALT GroupIrvine, California, United States

Est. 135,000 USD

About Balt Our purpose is to improve the lives of 150,000 patients in 2026. Our story Balt is a rapidly growing pioneer in an exceptional field. For 45 years, Balt has been leading the way - collaborating with physicians…

Full-time
BALT GroupIrvine, California, United States

Est. 95,000 USD

About Balt Our purpose is to improve the lives of 150,000 patients in 2026. Our story Balt is a rapidly growing pioneer in an exceptional field. For 45 years, Balt has been leading the way - collaborating with physicians…

Full-time
BALT GroupRemote

Est. 165,000 USD

About Balt Our purpose is to improve the lives of 150,000 patients in 2026. Our story Balt is a rapidly growing pioneer in an exceptional field. For 45 years, Balt has been leading the way - collaborating with physicians…

Full-timeRemote
Sr Data Engineer29 days ago
BALT GroupIrvine, California, United States

Est. 140,000 USD

This is an On-site Role in Irvine California About Balt Our purpose is to improve the lives of 150,000 patients in 2026. Our story Balt is a rapidly growing pioneer in an exceptional field. For 45 years, Balt has been le…

Full-time
BALT GroupBoston, Massachusetts, United States

Est. 125,000 USD

About Balt Our purpose is to improve the lives of 150,000 patients in 2026. Our story Balt is a rapidly growing pioneer in an exceptional field. For 45 years, Balt has been leading the way - collaborating with physicians…

Full-time
ClinChoiceCincinnati, Ohio, United States

Est. 85,000 USD

ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative “one-team” culture. We are looking for a dynamic person to…

Full-time
AtriCureMason, Ohio, United States

Est. 118,000 USD

AtriCure, Inc. provides innovative technologies for the treatment of Afib and related conditions. Afib affects more than 33 million people worldwide. Electrophysiologists and cardiothoracic surgeons around the globe use…

Full-time
KardiganSouth San Francisco, California, United States

Est. 200,000 USD

About Us Kardigan is a heart health company working to make cardiovascular disease preventable, curable and no longer the leading cause of death in the world. It is Kardigan’s mission to develop multiple targeted treatme…

Full-time
HeartflowSan Francisco, California, United States

Est. 215,000 USD

Heartflow is a medical technology company advancing the diagnosis and management of coronary artery disease, the #1 cause of death worldwide, using cutting-edge technology. The flagship product—an AI-driven, non-invasive…

Full-time
Arrowhead PharmaceuticalsPasadena, California, United States

Est. 190,000 USD

Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA…

Full-time
HeartflowAustin, Texas, United States

Est. 202,500 USD

Heartflow is a medical technology company advancing the diagnosis and management of coronary artery disease, the #1 cause of death worldwide, using cutting-edge technology. The flagship product—an AI-driven, non-invasive…

Full-time
HeartflowSan Francisco, California, United States

Est. 170,000 USD

Heartflow is a medical technology company advancing the diagnosis and management of coronary artery disease, the #1 cause of death worldwide, using cutting-edge technology. The flagship product—an AI-driven, non-invasive…

Full-time
AtriCureMason, Ohio, United States

Est. 94,500 USD

AtriCure, Inc. provides innovative technologies for the treatment of Afib and related conditions. Afib affects more than 33 million people worldwide. Electrophysiologists and cardiothoracic surgeons around the globe use…

Full-time
RevanceRemote

Est. 69,000 USD

Position Summary: The Regulatory Device Specialist prepares and submits high quality routine regulatory submissions to the FDA within company timelines and in accordance with regulatory guidelines and applicable federal…

Full-timeRemote
Acadia Pharmaceuticals Inc.Princeton, New Jersey, United States

Est. 173,500 USD

About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commerci…

Full-time
Personalis, IncFremont, California, United States

Est. 187,500 USD

At Personalis, we are transforming the active management of cancer through breakthrough personalized testing. We aim to drive a new paradigm for cancer management, guiding care from biopsy through the life of the patient…

Full-time
VaxcyteRemote

Est. 188,500 USD

Join our Mission to Protect Humankind! Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and co…

Full-timeRemote
HeartflowSan Francisco, California, United States

Est. 267,500 USD

Heartflow is a medical technology company advancing the diagnosis and management of coronary artery disease, the #1 cause of death worldwide, using cutting-edge technology. The flagship product—an AI-driven, non-invasive…

Full-time
Acadia Pharmaceuticals Inc.Princeton, New Jersey, United States

Est. 213,400 USD

About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commerci…

Full-time
Syner-GRemote

COMPANY DESCRIPTION: A career here is life-enhancing. At Syner-G, we enable our people to build careers that impact positively on their quality of life. Through our expertise, insight, consulting and management skills, w…

Full-timeRemote
Cambridge ConsultantsUnited Kingdom

Est. 55,000 GBP

Overview We’re looking for a Regulatory Affairs Specialist to join us, working across multidisciplinary teams to support and enable breakthrough innovation. Cambridge Consultants is a global technology and product develo…

Full-time
Acadia Pharmaceuticals Inc.Zug, Switzerland

About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commerci…

Full-time
Revolution MedicinesRedwood City, California, United States

Est. 209,500 USD

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress…

Full-time
Arrowhead PharmaceuticalsVerona, Wisconsin, United States

Est. 155,000 USD

Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA…

Full-time
Arrowhead PharmaceuticalsPasadena, California, United States

Est. 157,500 USD

Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA…

Full-time
Revolution MedicinesBasel, Basel-Stadt, Switzerland

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress…

Full-time